STANDARDS & METHOD

What we test, and against what.

Every claim on your assets is extracted, classified and ruled against four published rule sets. Nothing is judged on taste, and every finding names the standard it fails.

§ 01 — SEVERITY LADDER

Three tiers, defined by what they expose you to

Severity is not a measure of how strong a claim sounds. It is a measure of consequence — what happens if a regulator or a platform reads the sentence the way it is written.

CLASSIFICATION
CRITICAL

Names or implies a disease state, or asserts a clinical outcome. Warning-letter and listing-suppression exposure. Fix before anything else ships.

HIGH

Unsubstantiated efficacy or safety language. Defensible only with competent and reliable scientific evidence you can produce on request.

MEDIUM

Comparative, superlative or ranking language restricted by platform policy. Usually a wording change rather than a strategy change.

§ 02 — RULE SETS APPLIED

Four standards, applied to six asset types

FDA — structure/function boundary

Whether a claim describes an effect on normal structure or function, or crosses into diagnosing, treating, curing or preventing a condition. The boundary that turns a supplement into an unapproved drug.

FTC — substantiation

Whether the evidence you hold supports the claim as a consumer would read it, including the net impression of the page as a whole rather than each sentence in isolation.

Amazon — listing and A+ policy

Restricted claim categories, prohibited terms, and the specific language that triggers search suppression or ASIN takedown.

Meta — advertising standards

Personal-attribute and health-outcome rules that get ad accounts restricted, applied to live creative and to the email flows behind them.

ASSETS READ AMAZON LISTING · A+ CONTENT · PRODUCT PAGE · AD COPY · EMAIL FLOWS · AI ASSISTANT ANSWERS
§ 03 — THE SIXTH ASSET

Your claims are being restated by machines.

Shoppers increasingly ask an assistant which supplement to buy. The answer is assembled from your listing, your reviews and third-party coverage — and it routinely restates your careful structure/function language as a flat health claim.

It is still your claim. The same pharmacist judgement applies, and we read assistant answers about your product the same way we read your listing.

ASSISTANT ANSWER — EXTRACTTESTED

“…this supplement treats anxiety and improves sleep quality…”

Flagged: the assistant upgraded a compliant calm-support claim into a disease-treatment claim. The report shows which source passage caused it and the rewrite that stops it.

§ 04 — PROCESS

Five business days, four steps

01
02
03
04

You send links

We extract every claim

A pharmacist rules on each

You get the report

ASIN or product URL, plus access to whichever ad accounts and email flows you want in scope. About ten minutes of your time.

Each assertion is pulled from your live assets and classified. Extraction is machine-run, which is why the audit costs what it does.

Every severity rating and every rewrite is decided and signed by a licensed pharmacist. The judgement is not automated.

Findings, severities, rewrites and your peer benchmark. Formatted so a copywriter can implement it without interpretation.

§ 05 — SIGN-OFF

Who signs your report

REVIEWER OF RECORD
Reviewed and signed by a licensed pharmacist
CREDENTIAL — PHARMD
REGISTRATION — PROVINCIAL COLLEGE OF PHARMACISTS
IDENTITY — DISCLOSED ON ENGAGEMENT
REVIEW — EVERY FINDING, EVERY ENGAGEMENT
REGISTER ENTRY VERIFIABLE ON REQUEST

No finding leaves this office without a licensed pharmacist's signature on it.

Extraction surfaces candidate claims. A licensed pharmacist decides what each one actually asserts, what severity it carries, and whether the rewrite still says something you are willing to stand behind commercially.

That judgement is the difference between a keyword list and a review. It is also why the report is worth handing to a retailer, a broker or an acquirer.

We provide regulatory review of marketing language. We do not provide legal advice, and we do not represent you before any agency.
STANDING
Review standard
FDA · FTC · AMAZON · META
Findings retention
ENCRYPTED · DISCLOSED TO YOU ALONE
Reviewer register
VERIFIABLE ON REQUEST
ISO/IEC 17065
ACCREDITATION PLANNED FOR THE MARK